Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2024-05-14

FDA Approved: XELJANZ — Supplemental Application (Pfizer Laboratories Div Pfizer Inc)

View source ↗

Summary

FDA approved a supplemental application for XELJANZ (tofacitinib) from Pfizer, granting an additional regulatory action under NDA 213082.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • XELJANZ (tofacitinib)

Snippet

SUPPL AP for XELJANZ (TOFACITINIB)